Honeyborne Isobella, Prendergast Andrew, Pereyra Florencia, Leslie Alasdair, Crawford Hayley, Payne Rebecca, Reddy Shabashini, Bishop Karen, Moodley Eshia, Nair Kriebashnie, van der Stok Mary, McCarthy Noel, Rousseau Christine M, Addo Marylyn, Mullins James I, Brander Christian, Kiepiela Photini, Walker Bruce D, Goulder Philip J R
Department of Paediatrics, Peter Medawar Building for Pathogen Research, South Parks Road, Oxford OX1 3SY, United Kingdom.
J Virol. 2007 Apr;81(7):3667-72. doi: 10.1128/JVI.02689-06. Epub 2007 Jan 24.
To better understand relationships between CD8+ T-cell specificity and the immune control of human immunodeficiency virus type 1 (HIV-1), we analyzed the role of HLA-B13, an allele associated with low viremia, in a cohort of 578 C clade-infected individuals in Durban, South Africa. Six novel B13-restricted cytotoxic T lymphocyte epitopes were defined from analyses of 37 B13-positive subjects, including three Gag epitopes. These B13-restricted epitopes contribute to a broad Gag-specific CD8+ response that is associated with the control of viremia. These data are consistent with data from studies of other HLA-class I alleles associated with HIV control that have shown that the targeting of multiple Gag epitopes is associated with relative suppression of viremia.
为了更好地理解CD8 + T细胞特异性与人类免疫缺陷病毒1型(HIV-1)免疫控制之间的关系,我们分析了与低病毒血症相关的等位基因HLA-B13在南非德班578名C亚型感染个体队列中的作用。通过对37名B13阳性受试者的分析,确定了六个新的B13限制性细胞毒性T淋巴细胞表位,其中包括三个Gag表位。这些B13限制性表位促成了广泛的Gag特异性CD8 +反应,该反应与病毒血症的控制相关。这些数据与其他与HIV控制相关的HLA-I类等位基因的研究数据一致,这些研究表明,多个Gag表位的靶向与病毒血症的相对抑制有关。